Canonical Allele Identifier: CA1845638542

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648336A= , CM000671.2:g.34648336A=	GRCh38
NC_000009.11:g.34648333A= , CM000671.1:g.34648333A=	GRCh37
NC_000009.10:g.34638333A=	NCBI36
NG_009029.1:g.6699A=
NG_028966.1:g.1152A=
NG_009029.2:g.6748A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*155A=	ENSP00000509954.1:n.*155A=
ENST00000378842.8:c.567A= MANE Select	ENSP00000368119.4:p.Val189=
ENST00000378842.7:c.567A=	ENSP00000368119.3:p.Val189=
ENST00000450095.6:c.240A=	ENSP00000401956.2:p.Val80=
ENST00000472111.5:n.823A=
ENST00000473506.6:c.*155A=	ENSP00000432839.2:n.*155A=
ENST00000473529.5:n.726A=
ENST00000485531.1:n.1161A=
ENST00000487381.5:n.952A=
ENST00000489643.6:n.342A=
ENST00000554085.5:c.*311A=	ENSP00000450419.1:n.*311A=
ENST00000554139.5:n.813A=
ENST00000554550.5:c.*187A=	ENSP00000451435.1:n.*187A=
ENST00000554638.5:n.1039A=
ENST00000554897.5:c.*254A=	ENSP00000450942.1:n.*254A=
ENST00000554944.5:n.916A=
ENST00000555020.5:n.723A=
ENST00000555086.5:n.571A=
ENST00000555214.5:n.388A=
ENST00000556244.1:c.554A=
ENST00000556278.1:c.312A=	ENSP00000451792.1:p.Val104=
ENST00000556494.5:n.688A=
ENST00000557706.5:n.1129A=
NM_000155.3:c.567A=	NP_000146.2:p.Val189=
NM_001258332.1:c.240A=	NP_001245261.1:p.Val80=
NM_000155.4:c.567A= MANE Select	NP_000146.2:p.Val189=
NM_001258332.2:c.240A=	NP_001245261.1:p.Val80=